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CAS 1154579-82-4

:

2,3-Difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Description:
2,3-Difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound characterized by its pyridine ring substituted with two fluorine atoms at the 2 and 3 positions and a boron-containing moiety at the 5 position. The presence of the dioxaborolane group enhances its reactivity and solubility in various organic solvents, making it useful in synthetic chemistry, particularly in cross-coupling reactions. The fluorine substituents contribute to the compound's electronic properties, potentially influencing its reactivity and interaction with other molecules. This compound is of interest in medicinal chemistry and materials science due to its unique structural features. Additionally, the tetramethyl groups in the dioxaborolane enhance steric hindrance, which can affect the compound's stability and reactivity. Overall, 2,3-Difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile compound with potential applications in various fields of chemistry.
Formula:C11H14BF2NO2
InChI:InChI=1S/C11H14BF2NO2/c1-10(2)11(3,4)17-12(16-10)7-5-8(13)9(14)15-6-7/h5-6H,1-4H3
InChI key:InChIKey=VNZJHRDRAFSPLZ-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=C(F)C(F)=NC2
Synonyms:
  • 2,3-Difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2,3-Difluoro-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • Pyridine, 2,3-difluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2,3-Difluoropyridine-5-boronic acid pinacol ester
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